Dementia and Cognitive Neuroscience

Knight, M, McCann, B, Tsivos, D, Dillon, S, Coulthard, E & Kauppinen, R, 2016, ‘Quantitative T2 mapping of white matter: applications for ageing and cognitive decline’. Physics in Medicine and Biology, vol 61. Knight, M, McCann, B, Kauppinen, R & Coulthard, E, 2016, ‘Magnetic Resonance Imaging to Detect Early Molecular and Cellular Changes in Alzheimer’s Disease’. Frontiers in Aging Neuroscience, vol 8. Knight, M, McCann, B, Tsivos, D, Coulthard, E & Kauppinen, RA, 2016, ‘Quantitative T1 and T2 MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing’. Magnetic Resonance Materials in Physics, Biology and Medicine. Pennington, CM, Newson, M, Hayre, A & Coulthard, E, 2015, ‘Functional cognitive disorder: what is it and what to do about it?’. Pract Neurol. Pennington, CM, Hayre, A, Newson, M & Coulthard, E, 2015, ‘Functional Cognitive Disorder: A Common Cause of Subjective Cognitive Symptoms’. J Alzheimers Dis. Knight, M, Wood, B, Coulthard, L & Kauppinen, R, 2015, ‘Anisotropy of spin-echo T2 relaxation by magnetic resonance imaging in the human brain in vivo’. Biomedical Spectroscopy and Imaging. Archer, HA, Newson, MA & Coulthard, EJ, 2015, ‘Subjective Memory Complaints: Symptoms and Outcome in Different Research Settings’. J Alzheimers Dis, vol 48 Suppl 1., pp. S109-14 Kauppinen, RA, Wood, BJ, Knight, MJ, Tsivos, D & Coulthard, EJ, 2015, ‘Magnetic resonance scanning and image segmentation procedure at 3 T for volumetry of human hippocampal subfields’. Biomedical Spectroscopy and Imaging, vol 4., pp. 197-208 Archer, HA, Smailagic, N, John, C, Holmes, RB, Takwoingi, Y, Coulthard, EJ & Cullum, S, 2015, ‘Regional Cerebral Blood Flow Single Photon Emission Computed Tomography for detection of Frontotemporal dementia in people with suspected dementia’. Cochrane Database of Systematic Reviews, vol 6., pp. CD010896 Damseh, N, Danson, CM, Al-Ashhab, M, Abu-Libdeh, B, Gallon, M, Sharma, K, Yaacov, B, Caldwell, MA, Edvardson, S, Cullen, PJ, Elpeleg, O & Coulthard, E, 2015, ‘A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration’. Neurogenetics, vol 16., pp. 215-21